Classifications

• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
  • C21D9/46—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
  • C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
  • C21D8/0205—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips of ferrous alloys
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
  • C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
  • C21D8/04—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips to produce plates or strips for deep-drawing
  • C21D8/0421—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips to produce plates or strips for deep-drawing characterised by the working steps
  • C21D8/0426—Hot rolling
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  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
  • C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
  • C21D8/04—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips to produce plates or strips for deep-drawing
  • C21D8/0421—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips to produce plates or strips for deep-drawing characterised by the working steps
  • C21D8/0436—Cold rolling
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
  • C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
  • C21D8/04—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips to produce plates or strips for deep-drawing
  • C21D8/0447—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips to produce plates or strips for deep-drawing characterised by the heat treatment
  • C21D8/0463—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips to produce plates or strips for deep-drawing characterised by the heat treatment following hot rolling
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/001—Ferrous alloys, e.g. steel alloys containing N
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/002—Ferrous alloys, e.g. steel alloys containing In, Mg, or other elements not provided for in one single group C22C38/001 - C22C38/60
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/005—Ferrous alloys, e.g. steel alloys containing rare earths, i.e. Sc, Y, Lanthanides
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/06—Ferrous alloys, e.g. steel alloys containing aluminium
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/12—Ferrous alloys, e.g. steel alloys containing tungsten, tantalum, molybdenum, vanadium, or niobium
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/14—Ferrous alloys, e.g. steel alloys containing titanium or zirconium
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
  • C22C38/22—Ferrous alloys, e.g. steel alloys containing chromium with molybdenum or tungsten
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
  • C22C38/24—Ferrous alloys, e.g. steel alloys containing chromium with vanadium
• • C—CHEMISTRY; METALLURGY
  • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
  • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
  • C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
  • C23C2/02—Pretreatment of the material to be coated, e.g. for coating on selected surface areas
• • C—CHEMISTRY; METALLURGY
  • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
  • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
  • C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
  • C23C2/02—Pretreatment of the material to be coated, e.g. for coating on selected surface areas
  • C23C2/022—Pretreatment of the material to be coated, e.g. for coating on selected surface areas by heating
  • C23C2/0224—Two or more thermal pretreatments
• • C—CHEMISTRY; METALLURGY
  • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
  • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
  • C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
  • C23C2/02—Pretreatment of the material to be coated, e.g. for coating on selected surface areas
  • C23C2/024—Pretreatment of the material to be coated, e.g. for coating on selected surface areas by cleaning or etching
• • C—CHEMISTRY; METALLURGY
  • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
  • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
  • C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
  • C23C2/04—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
  • C23C2/06—Zinc or cadmium or alloys based thereon
• • C—CHEMISTRY; METALLURGY
  • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
  • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
  • C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
  • C23C2/26—After-treatment
  • C23C2/28—Thermal after-treatment, e.g. treatment in oil bath
• • C—CHEMISTRY; METALLURGY
  • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
  • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
  • C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
  • C23C2/34—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the shape of the material to be treated
  • C23C2/36—Elongated material
  • C23C2/40—Plates; Strips
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D2211/00—Microstructure comprising significant phases
  • C21D2211/001—Austenite
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D2211/00—Microstructure comprising significant phases
  • C21D2211/002—Bainite
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D2211/00—Microstructure comprising significant phases
  • C21D2211/005—Ferrite
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D2211/00—Microstructure comprising significant phases
  • C21D2211/009—Pearlite
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31678—Of metal

Definitions

• the present invention relates to a high strength galvanized steel sheet, which is suitable for a member used in industrial fields of automobile, electricity, and the like, with excellent workability and a method for manufacturing the same.
• various multi phase high strength galvanized steel sheets e.g., a ferrite-martensite dual-phase steel (Dual-phase Steel) and a TRIP steel taking the advantage of the transformation induced plasticity (Transformation Induced Plasticity) of retained austenite phase, have been developed.
• a ferrite-martensite dual-phase steel e.g., a ferrite-martensite dual-phase steel (Dual-phase Steel) and a TRIP steel taking the advantage of the transformation induced plasticity (Transformation Induced Plasticity) of retained austenite phase
• PTLs 1 and 2 have proposed steel sheets with excellent elongation by specifying the chemical components and specifying the volume fractions of retained austenite phase and martensitic phase and methods for manufacturing the same.
• PTL 3 has proposed a steel sheet with excellent elongation by specifying the chemical components and, furthermore, specifying a special method for manufacturing the same.
• PTL 4 has proposed a steel sheet with excellent elongation by specifying the chemical components and specifying the volume fractions of ferrite phase, bainite phase, and retained austenite phase.
• the main purpose is to improve the elongation by taking the advantage of the transformation induced plasticity of retained austenite phase and, therefore, the stretch flangeability is not taken into consideration. Consequently, development of a high strength galvanized steel sheet having high elongation and high stretch flangeability in combination becomes an issue.
• the present invention provides a high strength galvanized steel sheet having high strength (tensile strength TS of 590 MPa or more) and exhibiting excellent workability (high elongation and high stretch flangeability) and a method for manufacturing the same.
• the present inventors performed intensive research to obtain a high strength galvanized steel sheet having high strength (tensile strength TS of 590 MPa or more) and exhibiting excellent workability (elongation and stretch flangeability) and found the following.
• the area fraction of each phase was controlled appropriately and, thereby, the compatibility between high elongation and high stretch flangeability was able to be ensured with respect to a steel sheet at each strength level, where the tensile strength TS was 590 MPa or more.
• a high strength galvanized steel sheet with excellent workability characterized by having a component composition containing C: 0.04% or more, and 0.15% or less, Si: 0.7% or more, and 2.3% or less, Mn: 0.8% or more, and 2.2% or less, P: 0.1% or less, S: 0.01% or less, Al: 0.1% or less, N: 0.008% or less, and the remainder composed of iron and incidental impurities on a percent by mass basis, and a microstructure including 70% or more of ferrite phase, 2% or more, and 10% or less of bainite phase, and 0% or more, and 12% or less of pearlite phase on an area fraction basis and 1% or more, and 8% or less of retained austenite phase on a volume fraction basis, wherein an average crystal grain diameter of ferrite is 18 ⁇ m or less and an average crystal grain diameter of retained austenite is 2 ⁇ m or less.
• the high strength galvanized steel sheet with excellent workability according to the above-described item [1] or item [2], characterized by further containing at least one type of element selected from Cr: 0.05% or more, and 1.2% or less, V: 0.005% or more, and 1.0% or less, and Mo: 0.005% or more, and 0.5% or less, on a percent by mass basis, as the component composition.
• the high strength galvanized steel sheet with excellent workability according to any one of the above-described items [1] to [3], characterized by further containing at least one type of element selected from Ti: 0.01% or more, and 0.1% or less, Nb: 0.01% or more, and 0.1% or less, B: 0.0003% or more, and 0.0050% or less, Ni: 0.05% or more, and 2.0% or less, and Cu: 0.05% or more, and 2.0% or less, on a percent by mass basis, as the component composition.
• the high strength galvanized steel sheet with excellent workability according to any one of the above-described items [1] to [4], characterized by further containing at least one type of element selected from Ca: 0.001% or more, and 0.005% or less and REM: 0.001% or more, and 0.005% or less, on a percent by mass basis, as the component composition.
• a method for manufacturing a high strength galvanized steel sheet with excellent workability characterized by including the steps of subjecting a steel slab having the component composition according to any one of the above-described items [1], [3], [4], and [5] to hot rolling, pickling, and cold rolling, performing heating to a temperature range of 650° C. or higher at an average heating rate of 8° C./s or more, followed by keeping in a temperature range of 750° C. to 900° C. for 15 to 600 s, performing cooling to a temperature range of 300° C. to 550° C. at an average cooling rate of 3° C./s to 80° C./s, followed by keeping in the temperature range of 300° C. to 550° C. for 10 to 200 s, and performing galvanization.
• a method for manufacturing a high strength galvanized steel sheet with excellent workability characterized by including the steps of subjecting a steel slab having the component composition according to any one of the above-described items [1], [3], [4], and [5] to hot rolling and pickling, performing heating to a temperature range of 650° C. or higher at an average heating rate of 8° C./s or more, followed by keeping in a temperature range of 750° C. to 900° C. for 15 to 600 s, performing cooling to a temperature range of 300° C. to 550° C. at an average cooling rate of 3° C./s to 80° C./s, followed by keeping in the temperature range of 300° C. to 550° C. for 10 to 200 s, and performing galvanization.
• high strength galvanized steel sheet refers to a galvanized steel sheet having a tensile strength TS of 590 MPa or more.
• galvanized steel sheets regardless of whether an alloying treatment is performed or not, steel sheets in which a zinc coating is applied to a steel sheet by a galvanization method are generically called galvanized steel sheets. That is, the galvanized steel sheets in the present invention include both galvanized steel sheets not subjected to an alloying treatment and galvanized steel sheets subjected to an alloying treatment.
• a high strength galvanized steel sheet having high strength (tensile strength TS of 590 MPa or more) and exhibiting excellent workability (high elongation and high stretch flangeability) is obtained.
• high strength galvanized steel sheet according to the present invention is applied to, for example, an automobile structural member, enhancement of fuel economy due to weight reduction of a car body can be facilitated. Therefore, an industrial utility value is very large.
• the present inventors further performed research on utilization of a retained austenite phase and utilization of a pearlite phase and performed detailed research taking note of the possibility of improvement in characteristics of a multi phase composed of the ferrite phase, the bainite phase, the pearlite phase, the martensitic phase, and the retained austenite phase.
• compatibility between high elongation and high stretch flangeability was able to be ensured by intentional addition of Si for the purpose of solution hardening of a ferrite phase and an improvement of a work hardening property of the ferrite phase, reduction in hardness difference between different phases through formation of the multi phase composed of the ferrite phase, the bainite phase, the pearlite phase, the martensitic phase, and the retained austenite phase, and furthermore, optimization of the area of the multi phase.
• a component composition contains C: 0.04% or more, and 0.15% or less, Si: 0.7% or more, and 2.3% or less, Mn: 0.8% or more, and 2.2% or less, P: 0.1% or less, S: 0.01% or less, Al: 0.1% or less, N: 0.008% or less, and the remainder composed of iron and incidental impurities on a percent by mass basis
• a microstructure includes 70% or more of ferrite phase, 2% or more, and 10% or less of bainite phase, and 0% or more, and 12% or less of pearlite phase on an area fraction basis and includes 1% or more, and 8% or less of retained austenite phase on a volume fraction basis, an average crystal grain diameter of ferrite is 18 ⁇ m or less, and an average crystal grain diameter of retained austenite is 2 ⁇ m or less.
• Carbon is an austenite forming element and is an element effective in forming a multi phase and improving a balance between the strength and the elongation. If the amount of C is less than 0.04%, it is difficult to ensure a required amount of retained ⁇ and a bainite area fraction. On the other hand, if the amount of C exceeds 0.15% and, therefore, addition is excessive, the area fraction of hard martensitic phase exceeds 5%, and the stretch flangeability is degraded. Furthermore, a welded zone and a heat-affected zone are hardened significantly, and the mechanical characteristics of the welded zone are degraded. Therefore, C is specified to be 0.04% or more, and 0.15% or less, and preferably 0.05% or more, and 0.13% or less.
• Silicon is a ferrite forming element and is also an element effective in solution hardening.
• 0.7% or more of addition is preferred to improve a balance between the strength and the elongation and ensure the strength of the ferrite phase.
• 0.7% or more of addition is also preferred to ensure the retained austenite phase stably.
• excessive addition of Si causes degradation of surface properties due to an occurrence of red scale and the like, and degradation of deposition and adhesion. Therefore, Si is specified to be 0.7% or more, and 2.3% or less, and preferably 1.0% or more, and 1.8% or less.
• Manganese is an element effective in strengthening a steel. Furthermore, Mn is an element to stabilize austenite and an element preferred for adjusting the fraction of a secondary phase. For this purpose, addition of 0.8% or more of Mn is preferred. On the other hand, if addition is excessive and exceeds 2.2%, the fraction of the secondary phase becomes excessive and it becomes difficult to ensure the ferrite area fraction. Moreover, an increase in cost is brought about because an alloy cost of Mn has increased in recent years. Therefore, Mn is specified to be 0.8% or more, and 2.2% or less, and preferably 1.0% or more, and 2.0% or less.
• Phosphorus is an element effective in strengthening a steel. However, if addition is excessive and exceeds 0.1%, embrittlement is caused by grain boundary segregation, and an anti-crash property is degraded. Furthermore, if 0.1% is exceeded, an alloying speed is reduced significantly. Therefore, P is specified to be 0.1% or less.
• Sulfur forms inclusions, e.g., MnS, to cause degradation in anti-crash property and cracking along a metal flow of a welded zone and, therefore, is minimized, although S is specified to be 0.01% or less from the viewpoint of production cost.
• the amount of addition is specified to be 0.01% or more because if the amount is less than 0.01%, a large number of coarse oxides of Mn, Si, and the like are dispersed in the steel to degrade the material properties.
• the amount of Al exceeding 0.1% leads to degradation of surface properties. Therefore, the amount of Al is specified to be 0.1% or less, and preferably 0.01% to 0.1%.
• Nitrogen is an element which degrades the aging resistance of a steel to a greatest extent and preferably is minimized. If 0.008% is exceeded, degradation of the aging resistance becomes significant. Therefore, N is specified to be 0.008% or less.
• the remainder is composed of iron and incidental impurities. However, besides these component elements, the following alloy elements can be added.
• Chromium, vanadium, and molybdenum have a function of controlling generation of pearlite during cooling from an annealing temperature and, therefore, can be added.
• the effect thereof is obtained when Cr: 0.05% or more, V: 0.005% or more, and Mo: 0.005% or more are employed.
• Cr, V, and Mo are added in such a way as to exceed Cr: 1.2%, V: 1.0%, and Mo: 0.5%, respectively, the secondary layer fraction becomes too large, and degradation in stretch flangeability and the like may occur. Furthermore, an increase in cost is brought about. Therefore, in the case where these elements are added, each of the amounts thereof is specified to be Cr: 1.2% or less, V: 1.0% or less, or Mo: 0.5% or less.
• At least one type of element selected from Ti, Nb, B, Ni, and Cu described below can be contained.
• Ti 0.01% or more, and 0.1% or less
• Nb 0.01% or more, and 0.1% or less
• Titanium and niobium are effective in precipitation hardening of a steel. The effect is obtained when each of them is 0.01% or more and, therefore, there is no problem in use for strengthening the steel. However, if each of them exceeds 0.1%, the workability and the shape fixability are degraded. Furthermore, an increase in cost is brought about. Therefore, in the case where Ti and Nb are added, the amount of addition of Ti is specified to be 0.01% or more, and 0.1% or less and Nb is specified to be 0.01% or more, and 0.1% or less.
• B has a function of suppressing generation and growth of ferrite from austenite grain boundaries and, therefore, can be added.
• the effect is obtained when B is 0.0003% or more.
• B is specified to be 0.0003% or more, and 0.0050% or less.
• Ni 0.05% or More, and 2.0% or Less
• Cu 0.05% or More, and 2.0% or Less
• Nickel and copper are elements effective in strengthening a steel and there is no problem in use for strengthening the steel. Furthermore, internal oxidation is facilitated so as to improve adhesion of the coating. In order to obtain these effects, it is preferred that each of Ni and Cu is 0.05% or more. On the other hand, if both Ni and Cu, each exceeding 2.0%, are added, the workability of the steel sheet is degraded. Moreover, an increase in cost is brought about. Therefore, in the case where Ni and Cu are added, the amount of addition of each of them is specified to be 0.05% or more, and 2.0% or less.
• Calcium and REM are elements effective in spheroidizing the shape of a sulfide to improve an adverse influence of the sulfide on the stretch flangeability.
• each of Ca and REM is 0.001% or more.
• excessive addition causes increases in inclusions and the like so as to cause surface and internal defects. Therefore, in the case where Ca and REM are added, the amounts of addition of each of them is specified to be 0.001% or more, and 0.005% or less.
• a ferrite phase is 70% or more on an area fraction basis.
• a bainite phase is 2% or more on an area fraction basis.
• the bainite phase is specified to be 10% or less.
• the area fraction of bainite phase refers to a proportion of the area of a bainitic ferrite phase (ferrite having a high dislocation density) constituting an observation area.
• the pearlite phase is 12% or less on an area fraction basis.
• the pearlite which relaxes the hardness difference between soft ferrite and hard martensite and which has an intermediate hardness is 2% or more. Therefore, the pearlite phase is preferably 2% or more, and 10% or less.
• the retained austenite phase is 1% or more on a volume fraction basis. Meanwhile, in the case where the volume fraction of retained austenite phase exceeds 8%, a hard martensitic phase, which is generated through transformation of the retained austenite phase during stretch flange working, increases and, thereby, the stretch flangeability is degraded. Therefore, in order to ensure good stretch flangeability, it is preferred that the retained austenite phase is 8% or less on a volume fraction basis.
• the retained austenite phase is preferably 2% or more, and 6% or less.
• an average crystal grain diameter of ferrite is 18 ⁇ m or less. Meanwhile, in the case where the average crystal grain diameter of ferrite exceeds 18 ⁇ m, the dispersion state of secondary phases, which are present mostly at grain boundaries of ferrite, becomes dense locally, a microstructure, in which the secondary phase are dispersed uniformly, is not obtained, and degradation in stretch flangeability may occur.
• the average crystal grain diameter of retained austenite is 2 ⁇ m or less.
• a martensitic phase is 1% or more on an area fraction basis. Furthermore, in order to ensure good stretch flangeability, the area fraction of a hard martensitic phase is specified to be 5% or less.
• a tempered martensitic phase, a tempered bainite phase, and carbides, e.g., cementite, other than the ferrite phase, the pearlite phase, the bainite phase, the retained austenite phase, and the martensitic phase may be generated.
• the purpose of the present invention can preferably be achieved insofar as the above-described area fractions of the ferrite phase, pearlite phase and bainite phase, the volume fraction of the retained austenite phase, and the average crystal grain diameters of the ferrite and the retained austenite are satisfied.
• the area fractions of the ferrite phase, the bainite phase (bainitic ferrite phase), the pearlite phase, and the martensitic phase refers to proportions of the areas of the individual phases constituting an observation area.
• the high strength galvanized steel sheet according to embodiments of the present invention can be produced by a method in which a steel slab having the component composition conforming to the above-described component composition ranges is subjected to hot rolling, pickling, and cold rolling, heating to a temperature range of 650° C. or higher is performed at an average heating rate of 8° C./s or more, followed by keeping in a temperature range of 750° C. to 900° C. for 15 to 600 s, cooling to a temperature range of 300° C. to 550° C. is performed at an average cooling rate of 3° C./s to 80° C./s, followed by keeping in the temperature range of 300° C. to 550° C. for 10 to 200 s, galvanization is performed and, as necessary, an alloying treatment of zinc coating can be performed in a temperature range of 520° C. to 600° C.
• the above description relates to the case where a substrate steel sheet of the coating is a cold-rolled steel sheet, although the substrate steel sheet of the coating can also be a steel sheet after being subjected to the above-described hot rolling and pickling.
• a steel having the above-described component composition is melted, is made into a slab through roughing or continuous casting, and is made into a hot coil through hot rolling by a usually known process.
• the condition is not specifically limited, although it is preferable that the slab is heated to 1,100° C. to 1,300° C., hot rolling is performed at a final finishing temperature of 850° C. or higher, and steel sheet in coil is taken up at 400° C. to 750° C.
• the take-up temperature exceeds 750° C.
• carbides in the hot-rolled sheet may become coarse, and required strength cannot be obtained in some cases because such coarse carbides are not melted completely during soaking in short-time annealing and the like after hot rolling and pickling or after cold rolling.
• a pretreatment e.g., pickling and debinding
• cold rolling is performed by usually known method and, then, cold rolling is performed.
• the condition thereof is not necessarily specifically limited, although it is preferable that the cold rolling is performed under the cold reduction ratio of 30% or more. This is because if the cold reduction ratio is low, in some cases, recrystallization of ferrite is not facilitated, unrecrystallized ferrite remains, and the elongation and the stretch flangeability are degraded.
• the temperature range of heating is lower than 650° C. or the average heating rate is less than 8° C./s
• a fine uniformly dispersed austenite phase is not generated during annealing, a microstructure in which a secondary phases are locally concentratively present in a final microstructure is formed, and it is difficult to ensure good stretch flangeability.
• the average heating rate is less than 8° C./s
• a furnace longer than a usual furnace is necessary and, thereby, an increase in cost associated with large energy consumption and reduction in production efficiency are brought about.
• DFF Direct Fired Furnace
• DFF Direct Fired Furnace
• annealing for the purpose of annealing, keeping in a temperature range of 750° C. to 900° C., specifically in a single phase region of austenite or in a two-phase region of an austenite phase and a ferrite phase, is performed for 15 to 600 s.
• the annealing temperature is lower than 750° C. or the annealing time is less than 15 s, hard cementite in the steel sheet is not melted sufficiently in some cases, recrystallization of ferrite is not completed, and it becomes difficult to ensure a desired volume fraction of retained austenite phase, so that the elongation is degraded. Meanwhile, in the case where the annealing temperature exceeds 900° C.
• austenite becomes coarse during annealing and immediately after termination of cooling, most of the secondary phase becomes untransformed austenite in which C is thin. Consequently, in the downstream step of keeping in the temperature range of 300° C. to 550° C. for 10 to 200 s, bainite transformation proceeds so as to generate bainite containing carbides to a great extent, a martensitic phase and a retained austenite phase are hardly ensured, and it becomes difficult to ensure desired strength and good elongation. Moreover, an increase in cost associated with large energy consumption may be brought about.
• the average cooling rate is less than 3° C./s, most of the secondary phase is converted to pearlite or cementite during cooling, and finally, retained austenite phase can hardly be ensured, so that the elongation is degraded.
• the average cooling rate exceeds 80° C./s, generation of ferrite is not sufficient, a desired ferrite area fraction is not obtained, and the elongation is degraded.
• an upper limit of the average cooling rate is specified to be 15° C./s from the viewpoint of obtainment of a desired microstructure.
• the cooling termination temperature is lower than 300° C.
• bainite transformation is not facilitated, and a microstructure in which a bainite phase and a retained austenite phase are hardly present results, so that desired elongation is not obtained.
• the cooling termination temperature exceeds 550° C.
• most of the untransformed austenite is converted to cementite or pearlite, and it becomes difficult to obtain aimed area fraction of bainite phase and volume fraction of retained austenite phase, so that the elongation is degraded.
• the keeping temperature is lower than 300° C. or exceeds 550° C. or the case where the keeping time is less than 10 s, bainite transformation is not facilitated, and a microstructure in which a bainite phase and a retained austenite phase are hardly present results, so that desired elongation is not obtained. Furthermore, in the case where the keeping time exceeds 200 s, bainite transformation is facilitated excessively and, thereby, most of the secondary phase is converted to a bainite phase and cementite. Consequently, a final microstructure becomes a microstructure which hardly contains martensite and it becomes difficult to ensure desired strength.
• the steel sheet is dipped into a coating bath at a usual bath temperature so as to perform galvanization, and the amount of deposition is adjusted through gas wiping or the like.
• the surface is subjected to a galvanizing treatment.
• galvannealing is used frequently, wherein a heat treatment is performed after coating so as to diffuse Fe in the steel sheet into the coating layer. It is advantageous in the present invention that an alloying treatment of zinc coating is performed in this temperature range.
• a final microstructure becomes a microstructure in which a ferrite phase, a pearlite phase, and a bainite phase constitute most part and a retained austenite phase and a martensitic phase are hardly present, and it becomes difficult to ensure desired strength and good elongation.
• the alloying treatment temperature is lower than 520° C.
• untransformed austenite which contains a small amount of solid solution C is finally transformed to martensite while the amount of conversion to pearlite is small.
• the final microstructure is formed from the ferrite phase, the bainite phase, the retained austenite phase, and 5% or more of martensitic phase, different phase interfaces, at which a hardness difference between the above-described soft ferrite phase and the hard martensitic phase is large, increase significantly, and the stretch flangeability is degraded.
• the alloying treatment is performed in a high temperature range of 520° C. to 600° C.
• the configuration of the final microstructure is specified to be the ferrite phase, the pearlite phase, the bainite phase, the retained austenite phase, and a small amount, 5% or less, of martensitic phase, so that it becomes possible to further improve the stretch flangeability while good elongation is ensured.
• the temperature range of the alloying treatment is in the range of 540° C. to 590° C. in order to ensure the compatibility between good elongation and good stretch flangeability.
• the keeping temperature is not necessary constant insofar as the temperature is in the above-described range. Furthermore, even in the case where the cooling rate is changed during cooling, the gist of the present invention is not impaired insofar as the rate is in the specified range.
• the steel sheet may be subjected to a heat treatment by any equipment insofar as only the heat history is satisfied.
• the steel sheet is subjected to temper rolling after the heat treatment for the purpose of shape correction.
• a steel raw material is produced through usual steps of steel making, casting, and hot rolling. However, the steel raw material may be produced through thin wall casting or the like, where a part of or whole hot rolling step is omitted.
• the resulting slab was heated to 1,200° C., hot rolling to a sheet thickness of 3.2 mm was performed at a finish temperature of 870° C. to 920° C., and take up was performed at 520° C. Subsequently, the resulting hot-rolled steel sheet was pickled. Thereafter, cold rolling was performed so as to produce a cold-rolled steel sheet. Then, cold-rolled steel sheet obtained as described above was subjected to an annealing treatment and a galvanizing treatment with a continuous galvanization line under the production condition shown in Table 2.
• a galvannealing treatment including a heat treatment at 520° C. to 600° C. was further performed, so as to obtain a galvannealed steel sheet.
• a galvannealing treatment including a heat treatment at 520° C. to 600° C. was further performed, so as to obtain a galvannealed steel sheet.
• galvanized steel sheets not subjected to a galvannealing treatment were produced.
• the resulting slab was heated to 1,200° C., hot rolling to a predetermined sheet thickness was performed at a finish temperature of 870° C. to 920° C., and take up was performed at 520° C. Subsequently, the resulting hot-rolled steel sheet was pickled. Thereafter, an annealing treatment and a galvanizing treatment were performed with a continuous galvanization line under the production condition shown in Table 3.
• a galvannealing treatment including a heat treatment at 520° C. to 600° C. was further performed, so as to obtain a galvannealed steel sheet.
• a galvannealing treatment including a heat treatment at 520° C. to 600° C. was further performed, so as to obtain a galvannealed steel sheet.
• galvanized steel sheets not subjected to a galvannealing treatment were produced.
• Cooling Average keeping Keeping time termina- temperature until dipping Heating Annealing tion until dipping into coating Alloying tempera- Heating tempera- Annealing Cooling tempera- into coating bath after tempera- Steel ture rate ture time rate ture bath after cooling ture No. type ° C. ° C./s ° C. s ° C./s ° C. cooling ° C. s ° C.
• Cooling Average keeping Keeping time termina- temperature until dipping Heating Annealing tion until dipping into coating Alloying tempera- Heating tempera- Annealing Cooling tempera- into coating bath after tempera- Steel ture rate ture time rate ture bath after cooling ture No. type ° C. ° C./s ° C. s ° C./s ° C. cooling ° C. s ° C.
• the area fractions of a ferrite phase, a bainite phase, a pearlite phase, and a martensitic phase were determined by polishing a sheet thickness cross-section parallel to a rolling direction of the steel sheet, followed by corroding with 3% nital, and observing 10 visual fields with SEM (scanning electron microscope) under a magnification of 2,000 times through the use of Image-Pro of Media Cybernetics, Inc.
• the average crystal grain diameter of ferrite was determined by determining areas of individual ferrite grains through the use of Image-Pro described above, calculating equivalent circle diameters, and averaging those values.
• the volume fraction of retained austenite phase was determined on the basis of integrated intensity of ferrite and austenite peaks of a face at one-quarter sheet thickness, where the steel sheet was polished up to the one-quarter face in the sheet thickness direction.
• incident X-rays X-ray diffractometer using Co—K ⁇ was used, the intensity ratios were determined with respect to all combinations of integrated intensities of peaks of ⁇ 200 ⁇ , ⁇ 220 ⁇ , and ⁇ 311 ⁇ faces of retained austenite phase and ⁇ 220 ⁇ , ⁇ 200 ⁇ , and ⁇ 211 ⁇ faces of ferrite phase, and the average value of them was taken as the volume fraction of retained austenite phase.
• the average crystal grain diameter of retained austenite was determined by observing 10 or more retained austenite with TEM (transmission electron microscope) and averaging the crystal grain diameters.
• a tensile test was performed on the basis of JIS Z2241 by using JIS No. 5 test piece, where sample was taken in such a way that a tensile direction becomes in the direction orthogonal to the rolling direction of the steel sheet, and TS (tensile strength) and El (total elongation) were measured.
• the stretch flangeability (hole expansion property) was measured.
• the stretch flangeability was measured on the basis of the Japan Iron and Steel Federation Standard JFST1001.
• Each of the resulting steel sheets was cut into 100 mm ⁇ 100 mm, and a hole having a diameter of 10 mm was punched with a clearance of 12% ⁇ 1% when sheet thickness ⁇ 2.0 mm and with a clearance of 12% ⁇ 2% when sheet thickness ⁇ 2.0 mm.
• critical hole expansion ratio ⁇ (%) ⁇ ( D f ⁇ D 0 )/ D 0 ⁇ 100
• D f represents a hole diameter (mm) when cracking occurred and D 0 represents an initial hole diameter (mm).
• JIS Z2201 No. 5 test piece was cut from each of the L direction (rolling direction), the D direction (direction at 45° with respect to the rolling direction), and the C direction (direction at 90° with respect to the rolling direction) of the galvanized steel sheet, and r L , r D , and r C , respectively, was determined on the basis of JIS Z2254, and the r value was calculated from the following formula (1).
• r value ( r L +2 r D +r C )/4 (1)
• a cylindrical drawing test was performed, and deep drawability was evaluated on the basis of a limit drawing ratio (LDR).
• LDR limit drawing ratio
• a cylindrical punch having a diameter of 33 mm was used for the test, and a mold with dice diameter: 33+3 ⁇ sheet thickness mm was used.
• the test was performed at a blank holder pressure: 1 ton and a forming speed of 1 mm/s.
• the sliding state of the surface was changed depending on the coating state and the like and, therefore, in order to avoid the influence of the sliding state on the test, the test was performed under a highly lubricating condition state while a polyethylene sheet was disposed between the sample and the dice.
• the blank diameter was changed at 1 mm pitch, and the ratio (D/d) of the blank diameter D, which was drawn without breaking, to the punch diameter d was taken as LDR.
• Every high strength galvanized steel sheet according to the present invention preferably has TS of 590 MPa and exhibits excellent elongation and stretch flangeability. Furthermore, TS ⁇ El ⁇ 20,000 MPa ⁇ % and the balance between the strength and the elongation is high. Therefore, it is clear that high strength galvanized steel sheet with excellent workability is obtained. On the other hand, regarding comparative examples, at least one of the strength, the elongation, and the stretch flangeability is poor.

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